WO2002002505A3 - Composes pour le traitement de la maladie d'alzheimer - Google Patents
Composes pour le traitement de la maladie d'alzheimer Download PDFInfo
- Publication number
- WO2002002505A3 WO2002002505A3 PCT/US2001/020852 US0120852W WO0202505A3 WO 2002002505 A3 WO2002002505 A3 WO 2002002505A3 US 0120852 W US0120852 W US 0120852W WO 0202505 A3 WO0202505 A3 WO 0202505A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- disease
- compounds
- treat alzheimer
- alzheimer
- treat
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/125—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/13—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/04—Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C215/22—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated
- C07C215/28—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated and containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
- C07C233/77—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
- C07C233/78—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/70—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups and doubly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/84—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups and doubly-bound oxygen atoms bound to the same carbon skeleton with the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C239/00—Compounds containing nitrogen-to-halogen bonds; Hydroxylamino compounds or ethers or esters thereof
- C07C239/08—Hydroxylamino compounds or their ethers or esters
- C07C239/20—Hydroxylamino compounds or their ethers or esters having oxygen atoms of hydroxylamino groups etherified
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
- C07C243/10—Hydrazines
- C07C243/22—Hydrazines having nitrogen atoms of hydrazine groups bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
- C07C243/24—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids
- C07C243/26—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C243/28—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms to hydrogen atoms or to carbon atoms of a saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/16—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by singly-bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/18—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by doubly-bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/04—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms
- C07C275/20—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms of an unsaturated carbon skeleton
- C07C275/24—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/03—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/03—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C311/05—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms to acyclic carbon atoms of hydrocarbon radicals substituted by nitrogen atoms, not being part of nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/08—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/12—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings
- C07C311/13—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings the carbon skeleton containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/16—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/37—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/44—Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/50—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
- C07C323/51—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/60—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton with the carbon atom of at least one of the carboxyl groups bound to nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/60—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/12—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/04—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/36—Compounds containing oxirane rings with hydrocarbon radicals, substituted by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/52—Radicals substituted by nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/24—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Urology & Nephrology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Psychiatry (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicinal Preparation (AREA)
- Epoxy Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE60112942T DE60112942T2 (de) | 2000-06-30 | 2001-06-29 | Verbindungen zur behandlung der alzheimerischen krankheit |
| AT01950719T ATE302751T1 (de) | 2000-06-30 | 2001-06-29 | Verbindungen zur behandlung der alzheimerischen krankheit |
| EP01950719A EP1299349B1 (fr) | 2000-06-30 | 2001-06-29 | Composes pour le traitement de la maladie d'alzheimer |
| JP2002507762A JP2004502664A (ja) | 2000-06-30 | 2001-06-29 | アルツハイマー病処置用化合物 |
| CA002410680A CA2410680A1 (fr) | 2000-06-30 | 2001-06-29 | Composes pour le traitement de la maladie d'alzheimer |
| AU2001271686A AU2001271686A1 (en) | 2000-06-30 | 2001-06-29 | Compounds to treat alzheimer's disease |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US21532300P | 2000-06-30 | 2000-06-30 | |
| US60/215,323 | 2000-06-30 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| WO2002002505A2 WO2002002505A2 (fr) | 2002-01-10 |
| WO2002002505A3 true WO2002002505A3 (fr) | 2002-08-01 |
| WO2002002505A8 WO2002002505A8 (fr) | 2003-11-20 |
Family
ID=22802522
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2001/020930 Ceased WO2002002506A2 (fr) | 2000-06-30 | 2001-06-29 | Composes pour traiter la maladie d'alzheimer |
| PCT/US2001/020856 Ceased WO2002002518A2 (fr) | 2000-06-30 | 2001-06-29 | Composes pour traiter la maladie d'alzheimer |
| PCT/US2001/020852 Ceased WO2002002505A2 (fr) | 2000-06-30 | 2001-06-29 | Composes pour le traitement de la maladie d'alzheimer |
Family Applications Before (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2001/020930 Ceased WO2002002506A2 (fr) | 2000-06-30 | 2001-06-29 | Composes pour traiter la maladie d'alzheimer |
| PCT/US2001/020856 Ceased WO2002002518A2 (fr) | 2000-06-30 | 2001-06-29 | Composes pour traiter la maladie d'alzheimer |
Country Status (15)
| Country | Link |
|---|---|
| US (2) | US7034182B2 (fr) |
| EP (2) | EP1299352B1 (fr) |
| JP (2) | JP2004502665A (fr) |
| KR (1) | KR20030058959A (fr) |
| CN (1) | CN1217920C (fr) |
| AT (2) | ATE314343T1 (fr) |
| AU (3) | AU2001271686A1 (fr) |
| BR (1) | BR0111980A (fr) |
| CA (2) | CA2410680A1 (fr) |
| DE (2) | DE60112942T2 (fr) |
| ES (2) | ES2252257T3 (fr) |
| MX (1) | MXPA02012560A (fr) |
| NZ (1) | NZ523005A (fr) |
| WO (3) | WO2002002506A2 (fr) |
| ZA (2) | ZA200209991B (fr) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8691833B2 (en) | 2007-02-23 | 2014-04-08 | Merck Sharp & Dohme Corp. | Heterocyclic aspartyl protease inhibitors |
Families Citing this family (100)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20020276A1 (es) | 2000-06-30 | 2002-04-06 | Elan Pharm Inc | COMPUESTOS DE AMINA SUSTITUIDA COMO INHIBIDORES DE ß-SECRETASA PARA EL TRATAMIENTO DE ALZHEIMER |
| CA2410680A1 (fr) | 2000-06-30 | 2002-01-10 | Elan Pharmaceuticals, Inc. | Composes pour le traitement de la maladie d'alzheimer |
| US6846813B2 (en) | 2000-06-30 | 2005-01-25 | Pharmacia & Upjohn Company | Compounds to treat alzheimer's disease |
| US6696488B2 (en) | 2000-08-11 | 2004-02-24 | The Brigham And Women's Hospital, Inc. | (Hydroxyethyl)ureas as inhibitors of alzheimer's β-amyloid production |
| AR035960A1 (es) | 2001-04-23 | 2004-07-28 | Elan Pharm Inc | Epoxidos sustituidos y procesos para prepararlos |
| CA2448084A1 (fr) | 2001-05-22 | 2002-11-28 | Elan Pharmaceuticals, Inc. | Composes ethylamine hydroxyles aza |
| CA2448834A1 (fr) | 2001-06-01 | 2002-12-12 | Elan Pharmaceuticals, Inc. | Derives d'hydroxyalkylamines comme inhibiteurs de beta-secratase et leurs utilisations pour le traitement de la maladie d'alzheimer et de maladies similaires |
| MXPA04000140A (es) | 2001-06-27 | 2004-06-03 | Elan Pharm Inc | Derivados de beta-hidroxiamina utiles en el tratamiento de enfermedad de alzheimer. |
| CA2483959A1 (fr) * | 2001-08-28 | 2003-03-13 | Elan Pharmaceuticals, Inc. | Procede pour traiter la maladie d'alzheimer en utilisant les derives de quinaldoyl amine des hydrocarbures substitues par oxo- et hydroxy- |
| IL161881A0 (en) | 2001-11-08 | 2005-11-20 | Upjohn Co | N,N'-substituted-1,3-diamino-2-hydroxypropane derivatives |
| CA2467798A1 (fr) * | 2001-11-19 | 2003-05-30 | Pharmacia & Upjohn Company | Composes amine 1,2- et 1,3-diol et leur utilisation dans le traitement de la maladie d'alzheimer |
| CA2469130A1 (fr) * | 2001-12-04 | 2003-06-12 | Elan Pharmaceuticals, Inc. | Isosteres peptidiques contenant un heterocycle qui convient pour le traitement de la maladie d'alzheimer |
| BR0214736A (pt) * | 2001-12-06 | 2004-11-23 | Elan Pharm Inc | Composto e seus sais farmaceuticamente aceitáveis, composição farmacêutica e método de tratar seres humanos ou animais que sofrem de doenças ou condições |
| CA2471531A1 (fr) * | 2001-12-26 | 2003-07-10 | Takeda Chemical Industries, Ltd. | Remedes contre les troubles cognitifs legers |
| US7132568B2 (en) | 2002-06-17 | 2006-11-07 | Sunesis Pharmaceuticals, Inc. | Aspartyl protease inhibitors |
| US7115652B2 (en) | 2002-06-17 | 2006-10-03 | Sunesis Pharmaceuticals, Inc. | Aspartyl protease inhibitors |
| US7459476B2 (en) | 2002-06-27 | 2008-12-02 | Elan Pharmaceuticals, Inc. | Methods for treating Alzheimer's disease using hydroxyethylene compounds containing a heterocyclic amide bond isostere |
| US7557137B2 (en) * | 2002-08-05 | 2009-07-07 | Bristol-Myers Squibb Company | Gamma-lactams as beta-secretase inhibitors |
| AU2003266967B2 (en) * | 2002-08-07 | 2006-11-16 | Novartis Ag | Methods for the treatment of dementia based on Apo E genotype |
| WO2004014843A1 (fr) * | 2002-08-09 | 2004-02-19 | Takeda Chemical Industries, Ltd. | Composés amino substitués et utilisation de ces composés |
| NZ538625A (en) * | 2002-09-06 | 2008-05-30 | Pharmacia & Upjohn Co Llc | 1,3-Diamino-2-hydroxypropane prodrug derivatives |
| JP2005538177A (ja) * | 2002-09-10 | 2005-12-15 | ファルマシア・アンド・アップジョン・カンパニー・エルエルシー | アルツハイマー病処置用置換アミノエーテル化合物 |
| UY27967A1 (es) * | 2002-09-10 | 2004-05-31 | Pfizer | Acetil 2-hindroxi-1,3-diaminoalcanos |
| US7109217B2 (en) | 2002-11-12 | 2006-09-19 | Merck & Co., Inc. | Phenylcarboxamide beta-secretase inhibitors for the treatment of Alzheimer's disease |
| DOP2003000765A (es) * | 2002-11-27 | 2004-05-31 | Elan Fharmaceuticals Inc | Ureas substituidas y carbamatos utiles para el tratamiento de la enfermedad de alzheimer (substituted ureas and carbamates useful in the treatment of alzheimer`s disease |
| GB0228410D0 (en) | 2002-12-05 | 2003-01-08 | Glaxo Group Ltd | Novel Compounds |
| US7521481B2 (en) | 2003-02-27 | 2009-04-21 | Mclaurin Joanne | Methods of preventing, treating and diagnosing disorders of protein aggregation |
| GB0305918D0 (en) * | 2003-03-14 | 2003-04-23 | Glaxo Group Ltd | Novel compounds |
| CA2523232A1 (fr) * | 2003-04-21 | 2004-11-04 | Elan Pharmaceuticals, Inc. | Benzamide 2-hydroxy-3-diaminoalcanes |
| JP2006524258A (ja) * | 2003-04-21 | 2006-10-26 | イーラン ファーマスーティカルズ、インコーポレイテッド | フェナシル2−ヒドロキシ−3−ジアミノアルカン |
| GB0309221D0 (en) * | 2003-04-23 | 2003-06-04 | Glaxo Group Ltd | Novel compounds |
| AU2004255183A1 (en) * | 2003-06-30 | 2005-01-20 | Merck & Co., Inc. | N-alkyl phenylcarboxamide beta-secretase inhibitors for the treatment of Alzheimer's disease |
| DE602004015476D1 (de) | 2003-08-08 | 2008-09-11 | Schering Corp | Cyclische amine mit einem heterocyclischen substituenten als bace-1-inhibitoren |
| WO2005016876A2 (fr) | 2003-08-08 | 2005-02-24 | Schering Corporation | Inhibiteurs bace-1 amines cycliques a substituant benzamide |
| GB0328900D0 (en) * | 2003-12-12 | 2004-01-14 | Glaxo Group Ltd | Novel compounds |
| US7592348B2 (en) | 2003-12-15 | 2009-09-22 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| US7700603B2 (en) | 2003-12-15 | 2010-04-20 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| FR2866647B1 (fr) * | 2004-02-20 | 2006-10-27 | Servier Lab | Nouveaux derives azabicycliques, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| US7544717B2 (en) * | 2004-03-25 | 2009-06-09 | Elan Pharmaceuticals, Inc. | 2-amino- and 2-thio- substituted 1,3-diaminopropanes |
| WO2006014762A1 (fr) | 2004-07-22 | 2006-02-09 | Schering Corporation | Inhibiteurs d'amide beta secretase substitues |
| CA2575340A1 (fr) | 2004-07-28 | 2006-02-09 | Schering Corporation | Inhibiteurs de beta-secretase macrocycliques |
| US7361789B1 (en) | 2004-07-28 | 2008-04-22 | Amgen Inc. | Dihydronaphthalene compounds, compositions, uses thereof, and methods for synthesis |
| US20080207527A1 (en) * | 2004-09-17 | 2008-08-28 | Comentis, Inc. | Bicyclic Compounds Which Inhibit Beta-Secretase Activity and Methods of Use Thereof |
| WO2006032999A1 (fr) | 2004-09-21 | 2006-03-30 | Pfizer Products Inc. | N-methyl hydroxyethylamine utile dans le traitement d'affections du systeme nerveux central |
| US20070213368A1 (en) * | 2004-09-21 | 2007-09-13 | Kleinman Edward F | N-ethyl hydroxyethylamine useful in treating cns conditions |
| US7745470B2 (en) | 2005-03-10 | 2010-06-29 | Bristol-Myers Squibb Company | Isophthalates as beta-secretase inhibitors |
| GB0506562D0 (en) * | 2005-03-31 | 2005-05-04 | Glaxo Group Ltd | Novel compounds |
| WO2006110668A1 (fr) * | 2005-04-08 | 2006-10-19 | Comentis, Inc. | Composes inhibant l'activite beta-secretase et leurs methodes d'utilisation |
| JPWO2007020888A1 (ja) | 2005-08-12 | 2009-02-26 | 武田薬品工業株式会社 | 脳・神経細胞保護剤および睡眠障害治療薬 |
| US7838676B2 (en) | 2005-11-21 | 2010-11-23 | Amgen Inc. | Beta-secretase modulators and methods of use |
| US7745484B2 (en) | 2005-11-21 | 2010-06-29 | Amgen Inc. | Beta-secretase modulators and methods of use |
| CA2629402C (fr) | 2005-11-21 | 2011-07-26 | Amgen Inc. | Modulateurs de beta-secretase et procedes d'utilisation associes |
| US7872009B2 (en) | 2005-11-21 | 2011-01-18 | Amgen Inc. | Beta-Secretase modulators and methods of use |
| PE20080145A1 (es) * | 2006-03-21 | 2008-02-11 | Janssen Pharmaceutica Nv | Tetrahidro-pirimidoazepinas como moduladores de trpv1 |
| WO2007110727A2 (fr) * | 2006-03-27 | 2007-10-04 | Pfizer Products Inc. | Hydroxyethylamines stabilisees par un amide |
| GB0607952D0 (en) * | 2006-04-21 | 2006-05-31 | Minster Res Ltd | Novel treatment |
| TW200815349A (en) | 2006-06-22 | 2008-04-01 | Astrazeneca Ab | New compounds |
| JP5379692B2 (ja) | 2006-11-09 | 2013-12-25 | プロビオドルグ エージー | 潰瘍、癌及び他の疾患の治療のためのグルタミニルシクラーゼの阻害薬としての3−ヒドロキシ−1,5−ジヒドロ−ピロール−2−オン誘導体 |
| EP2091948B1 (fr) | 2006-11-30 | 2012-04-18 | Probiodrug AG | Nouveaux inhibiteurs de glutaminylcyclase |
| CN101668751A (zh) | 2006-12-12 | 2010-03-10 | 先灵公司 | 天冬氨酰蛋白酶抑制剂 |
| JP2010518064A (ja) | 2007-02-12 | 2010-05-27 | メルク・シャープ・エンド・ドーム・コーポレイション | Adおよび関連状態の治療のためのピペラジン誘導体 |
| AU2008220785B2 (en) | 2007-03-01 | 2013-02-21 | Vivoryon Therapeutics N.V. | New use of glutaminyl cyclase inhibitors |
| WO2008128985A1 (fr) | 2007-04-18 | 2008-10-30 | Probiodrug Ag | Dérivés de thio-urée utilisés comme inhibiteurs de la glutaminyl cyclase |
| US8163909B2 (en) | 2007-05-25 | 2012-04-24 | Amgen Inc. | Substituted hydroxyethyl amine compounds as beta-secretase modulators and methods of use |
| ES2436364T3 (es) | 2007-05-25 | 2013-12-30 | Amgen Inc. | Compuestos de hidroxietilamina sustituidos como moduladores de beta-secretasa y métodos de uso |
| KR20100051668A (ko) * | 2007-07-26 | 2010-05-17 | 코멘티스, 인코포레이티드 | 베타-세크레타제 활성을 억제하는 이소프탈아미드 유도체 |
| US8299267B2 (en) | 2007-09-24 | 2012-10-30 | Comentis, Inc. | (3-hydroxy-4-amino-butan-2-yl) -3- (2-thiazol-2-yl-pyrrolidine-1-carbonyl) benzamide derivatives and related compounds as beta-secretase inhibitors for treating |
| SE531873C2 (sv) * | 2007-11-12 | 2009-09-01 | Lifeassays Ab | Anordning för biokemisk bearbetning och analys av provvätska |
| US7803809B2 (en) | 2008-11-12 | 2010-09-28 | Amgen Inc. | Substituted pyrano [2,3-b] pyridinamine compounds as beta-secretase modulators and methods of use |
| JP5562865B2 (ja) | 2007-12-17 | 2014-07-30 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Trpv1のイミダゾロ−、オキサゾロ−、及びチアゾロピリミジン・モジュレーター |
| US8461389B2 (en) | 2008-04-18 | 2013-06-11 | University College Dublin, National University Of Ireland, Dublin | Psycho-pharmaceuticals |
| DK2282779T3 (da) * | 2008-04-29 | 2013-05-27 | Pharnext | Nye terapeutiske fremgangsmåder til behandling af alzheimer sygdom og beslægtede lidelser gennem en modulation af cellestress-respons |
| EP3586839A1 (fr) | 2008-07-28 | 2020-01-01 | Blanchette Rockefeller Neurosciences, Institute | Composés d'activation de pkc pour le traitement de maladies neurodégénératives |
| CN102209721A (zh) * | 2008-09-11 | 2011-10-05 | 安姆根有限公司 | 作为β-分泌酶调节剂的螺四环化合物及其使用方法 |
| TW201020244A (en) | 2008-11-14 | 2010-06-01 | Astrazeneca Ab | New compounds |
| JP2012526840A (ja) * | 2009-05-13 | 2012-11-01 | プロテイン デリヴァリー ソリューションズ エルエルシー | 膜貫通送達のための製剤系 |
| EP2281824A1 (fr) | 2009-08-07 | 2011-02-09 | Noscira, S.A. | Dérivés de furan-imidazolone pour le traitement de maladies ou de troubles cognitifs, neurodégénératifs ou neuronaux |
| WO2011029920A1 (fr) | 2009-09-11 | 2011-03-17 | Probiodrug Ag | Dérivés hétérocycliques en tant qu'inhibiteurs de glutaminyle cyclase |
| EP2504315A1 (fr) | 2009-11-23 | 2012-10-03 | Amgen Inc. | Composés amino hétéroaryles comme modulateurs de la bêta-secrétase et procédés d'utilisation |
| US8822485B2 (en) | 2009-11-23 | 2014-09-02 | Amgen Inc. | Amino heteroaryl compounds as beta-secretase modulators and methods of use |
| EP2526092B1 (fr) | 2010-01-19 | 2014-08-06 | Amgen Inc. | Composés aminohétéroaryles comme modulators de la beta-secretase, et les procédés pour leur utilisation. |
| CA2788071A1 (fr) * | 2010-02-05 | 2011-08-11 | Pfizer Inc. | Composes d'uree a base de pyrrolo[2,3-d]pyrimidine a titre d'inhibiteurs de jak |
| EP2542549B1 (fr) | 2010-03-03 | 2016-05-11 | Probiodrug AG | Inhibiteurs de glutaminyl cyclase |
| AU2011226074B2 (en) | 2010-03-10 | 2015-01-22 | Vivoryon Therapeutics N.V. | Heterocyclic inhibitors of glutaminyl cyclase (QC, EC 2.3.2.5) |
| EP2547686B1 (fr) | 2010-03-15 | 2014-01-22 | Amgen Inc. | Composés spirannique de amino-dihydrooxazine et amino-dihydrothiazine comme modulateur de bêta-sécrétase et leur utilisation médicale |
| MX2012010658A (es) | 2010-03-15 | 2012-12-05 | Amgen Inc | Compuestos de anillo espiro tetraciclico como moduladores de beta-secretasa. |
| US8541596B2 (en) | 2010-04-21 | 2013-09-24 | Probiodrug Ag | Inhibitors |
| EP2643299B1 (fr) | 2010-11-22 | 2016-06-22 | Noscira, S.A. | Dérivés de bipyridine-sulfonamide pour le traitement de maladies et d'affections neurodégénératives |
| US9346827B2 (en) | 2011-02-07 | 2016-05-24 | Amgen Inc. | 5-amino-oxazepine and 5-amino-thiazepane compounds as beta secretase antagonists and methods of use |
| US8530670B2 (en) | 2011-03-16 | 2013-09-10 | Probiodrug Ag | Inhibitors |
| US9296759B2 (en) | 2011-09-21 | 2016-03-29 | Amgen Inc. | Amino-oxazine and amino-dihydrothiazine compounds as beta-secretase modulators and methods of use |
| WO2014078314A1 (fr) | 2012-11-15 | 2014-05-22 | Amgen Inc. | Composés d'amino-oxazine et d'amino-dihydrothiazine jouant le rôle de modulateurs de bêta-sécrétase et procédés d'utilisation |
| US9302992B2 (en) * | 2013-04-02 | 2016-04-05 | Annji Pharmaceutical Co., Ltd. | Multifunctional quinoline derivatives as anti-neurodegenerative agents |
| CN106748892B (zh) * | 2017-01-18 | 2018-09-18 | 四川大学 | 靶向自噬激动剂及其在神经退行性疾病治疗药物中的应用 |
| CN111108105B (zh) | 2017-09-22 | 2023-03-31 | 朱比兰特埃皮帕德有限公司 | 作为pad抑制剂的杂环化合物 |
| DK3461819T3 (da) | 2017-09-29 | 2020-08-10 | Probiodrug Ag | Inhibitorer af glutaminylcyklase |
| PL3697785T3 (pl) | 2017-10-18 | 2023-08-07 | Jubilant Epipad LLC | Związki imidazopirydynowe jako inhibitory pad |
| KR20200085836A (ko) | 2017-11-06 | 2020-07-15 | 주빌런트 프로델 엘엘씨 | Pd1/pd-l1 활성화 억제제로서의 피리미딘 유도체 |
| DK3704120T3 (da) | 2017-11-24 | 2024-05-21 | Jubilant Episcribe Llc | Heterocykliske forbindelser som prmt5-inhibitorer |
| EP3765453A1 (fr) | 2018-03-13 | 2021-01-20 | Jubilant Prodel LLC | Composés bicycliques utilisés en tant qu'inhibiteurs de l'interaction/activation de pd1/pd-l1 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0652009A1 (fr) * | 1993-08-09 | 1995-05-10 | Eli Lilly And Company | L'identification et l'utilisation des inhibiteurs de la protease aspartic |
| WO1998033795A1 (fr) * | 1997-02-04 | 1998-08-06 | The Regents Of The University Of California | Inhibiteurs de cathepsine d nanomolaires et non peptidiques |
Family Cites Families (153)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5753564Y2 (fr) | 1977-06-01 | 1982-11-19 | ||
| CH624011A5 (fr) | 1977-08-05 | 1981-07-15 | Battelle Memorial Institute | |
| FR2416008A1 (fr) | 1978-02-02 | 1979-08-31 | Oreal | Lyophilisats de liposomes |
| US4235871A (en) | 1978-02-24 | 1980-11-25 | Papahadjopoulos Demetrios P | Method of encapsulating biologically active materials in lipid vesicles |
| US4394448A (en) | 1978-02-24 | 1983-07-19 | Szoka Jr Francis C | Method of inserting DNA into living cells |
| US4399216A (en) | 1980-02-25 | 1983-08-16 | The Trustees Of Columbia University | Processes for inserting DNA into eucaryotic cells and for producing proteinaceous materials |
| ZA811368B (en) | 1980-03-24 | 1982-04-28 | Genentech Inc | Bacterial polypedtide expression employing tryptophan promoter-operator |
| US5142056A (en) | 1989-05-23 | 1992-08-25 | Abbott Laboratories | Retroviral protease inhibiting compounds |
| NZ201705A (en) | 1981-08-31 | 1986-03-14 | Genentech Inc | Recombinant dna method for production of hepatitis b surface antigen in yeast |
| US4522811A (en) | 1982-07-08 | 1985-06-11 | Syntex (U.S.A.) Inc. | Serial injection of muramyldipeptides and liposomes enhances the anti-infective activity of muramyldipeptides |
| US4870009A (en) | 1982-11-22 | 1989-09-26 | The Salk Institute For Biological Studies | Method of obtaining gene product through the generation of transgenic animals |
| US4668770A (en) | 1982-12-27 | 1987-05-26 | Merck & Co., Inc. | Renin inhibitory tripeptides |
| US4713339A (en) | 1983-01-19 | 1987-12-15 | Genentech, Inc. | Polycistronic expression vector construction |
| AU2353384A (en) | 1983-01-19 | 1984-07-26 | Genentech Inc. | Amplification in eukaryotic host cells |
| US4816567A (en) | 1983-04-08 | 1989-03-28 | Genentech, Inc. | Recombinant immunoglobin preparations |
| US4474778A (en) * | 1983-11-09 | 1984-10-02 | E. R. Squibb & Sons, Inc. | Lactam containing compounds, their pharmaceutical compositions and method of use |
| US4512988A (en) * | 1984-03-01 | 1985-04-23 | E. R. Squibb & Sons, Inc. | Acylamino oxo or hydroxy substituted alkylamino thiazines and thiazepines |
| US4636491A (en) | 1984-03-27 | 1987-01-13 | Merck & Co., Inc. | Renin inhibitory peptides having improved solubility |
| US4736866B1 (en) | 1984-06-22 | 1988-04-12 | Transgenic non-human mammals | |
| JPH0662529B2 (ja) | 1984-07-13 | 1994-08-17 | 三共株式会社 | アミノ酸誘導体 |
| US4880781A (en) | 1984-08-06 | 1989-11-14 | The Upjohn Company | Renin inhibitory peptides containing an N-alkyl-histidine moiety |
| JPS6150912A (ja) | 1984-08-16 | 1986-03-13 | Shionogi & Co Ltd | リポソ−ム製剤の製造法 |
| US4814270A (en) | 1984-09-13 | 1989-03-21 | Becton Dickinson And Company | Production of loaded vesicles |
| US4749792A (en) | 1984-09-26 | 1988-06-07 | E. R. Squibb & Sons, Inc. | Diamino ketones and alcohols as analgesic agents |
| US4616088A (en) | 1984-10-29 | 1986-10-07 | E. R. Squibb & Sons, Inc. | Amino acid ester and amide renin inhibitor |
| US4665193A (en) | 1984-12-14 | 1987-05-12 | E. R. Squibb & Sons, Inc. | Amino acid ester renin inhibitors |
| US4897355A (en) | 1985-01-07 | 1990-01-30 | Syntex (U.S.A.) Inc. | N[ω,(ω-1)-dialkyloxy]- and N-[ω,(ω-1)-dialkenyloxy]-alk-1-yl-N,N,N-tetrasubstituted ammonium lipids and uses therefor |
| US4753788A (en) | 1985-01-31 | 1988-06-28 | Vestar Research Inc. | Method for preparing small vesicles using microemulsification |
| CA1290097C (fr) | 1985-07-24 | 1991-10-01 | Merck & Co., Inc. | Inhibiteurs d'enzymes de type peptide |
| US4729985A (en) | 1985-08-09 | 1988-03-08 | Pfizer Inc. | Renin inhibitors containing 5-amino-2,5-disubstituted-4-hydroxypentanoic acid residues |
| US5175281A (en) | 1985-09-12 | 1992-12-29 | The Upjohn Company | Pharmaceutically active pyrimidinylpiperazinylsterioids |
| US4676980A (en) | 1985-09-23 | 1987-06-30 | The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | Target specific cross-linked heteroantibodies |
| WO1987002986A1 (fr) | 1985-11-15 | 1987-05-21 | The Upjohn Company | Nouveaux analogues de polypeptides inhibiteurs de renine contenant s-aryl-d-cysteinyle ou l-cysteinyle ou dl-cysteinyle, de l'acide 3-(arylthio) lactique ou des moities de 3-(arylthio)-alkyl |
| WO1987004349A1 (fr) | 1986-01-16 | 1987-07-30 | Joseph Dellaria | Analogues de peptides |
| JPS63502716A (ja) | 1986-03-07 | 1988-10-13 | マサチューセッツ・インステチュート・オブ・テクノロジー | 糖タンパク安定性の強化方法 |
| DE3610593A1 (de) | 1986-03-29 | 1987-10-01 | Hoechst Ag | Substituierte 4-amino-3-hydroxybuttersaeure-derivate verfahren zu deren herstellung, diese enthaltende mittel und ihre verwendung |
| EP0264106B1 (fr) | 1986-10-14 | 1994-03-16 | Banyu Pharmaceutical Co., Ltd. | Dérivés 5-substitués de l'acide amino-4-hydroxy-pentanoique et leur emploi |
| US4935405A (en) * | 1986-10-31 | 1990-06-19 | Pfizer Inc. | Nor-statine and nor-cyclostatine polypeptides |
| EP0274259B1 (fr) | 1986-12-19 | 1994-02-16 | Sankyo Company Limited | Oligopeptides inhibant la rénine, leur préparation et leur application |
| US5250565A (en) | 1987-02-10 | 1993-10-05 | Abbott Laboratories | Indole-,benzofuran-,and benzothiophene-containing lipoxygenase-inhibiting compounds |
| DE3721855A1 (de) | 1987-03-12 | 1988-09-22 | Merck Patent Gmbh | Aminosaeurederivate |
| FR2614533A1 (fr) | 1987-04-23 | 1988-11-04 | Sandoz Sa | Nouveaux derives peptidiques, leur preparation et leur utilisation comme medicaments |
| KR890701579A (ko) | 1987-06-29 | 1989-12-21 | 로버어트 에이 아미테이지 | 레닌 억제 펩타이드를 함유하는 말산 유도체 |
| US5010182A (en) | 1987-07-28 | 1991-04-23 | Chiron Corporation | DNA constructs containing a Kluyveromyces alpha factor leader sequence for directing secretion of heterologous polypeptides |
| WO1989001488A1 (fr) | 1987-08-07 | 1989-02-23 | The Upjohn Company | Peptides inhibiteurs de la renine a liaisons non peptidiques |
| GB8724885D0 (en) | 1987-10-23 | 1987-11-25 | Binns M M | Fowlpox virus promotors |
| GB8728561D0 (en) | 1987-12-07 | 1988-01-13 | Glaxo Group Ltd | Chemical compounds |
| DE3863357D1 (de) | 1987-12-16 | 1991-07-25 | Dallmer Gmbh & Co | Ablaufarmatur fuer einen fliesenfussboden. |
| WO1989005859A1 (fr) | 1987-12-21 | 1989-06-29 | The Upjohn Company | Transformation par l'agrobacterium de graines de plantes de germination |
| IL89900A0 (en) | 1988-04-12 | 1989-12-15 | Merck & Co Inc | Hiv protease inhibitors useful for the treatment of aids and pharmaceutical compositions containing them |
| AU4005289A (en) | 1988-08-25 | 1990-03-01 | Smithkline Beecham Corporation | Recombinant saccharomyces |
| DE3841520A1 (de) | 1988-12-09 | 1990-06-13 | Hoechst Ag | Enzymhemmende harnstoffderivate von dipeptiden, verfahren zu ihrer herstellung, diese enthaltende mittel und ihre verwendung |
| FR2646437B1 (fr) | 1989-04-28 | 1991-08-30 | Transgene Sa | Nouvelles sequences d'adn, leur application en tant que sequence codant pour un peptide signal pour la secretion de proteines matures par des levures recombinantes, cassettes d'expression, levures transformees et procede de preparation de proteines correspondant |
| EP0739904A1 (fr) | 1989-06-29 | 1996-10-30 | Medarex, Inc. | Réactifs bispécifiques pour le traitement du SIDA |
| GB8927915D0 (en) * | 1989-12-11 | 1990-02-14 | Hoffmann La Roche | Novel alcohols |
| DE3941235A1 (de) | 1989-12-14 | 1991-06-20 | Bayer Ag | Neue peptide, ihre herstellung und ihre verwendung in arzneimitteln |
| DE4001236A1 (de) | 1990-01-18 | 1991-07-25 | Bayer Ag | Neue peptide, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel, insbesondere als arzneimittel gegen retroviren |
| DE4003575A1 (de) | 1990-02-07 | 1991-08-08 | Bayer Ag | Retroisostere dipeptide, verfahren zur herstellung und ihre verwendung als renininhibitoren in arzneimitteln |
| GB9004483D0 (en) | 1990-02-28 | 1990-04-25 | Erba Carlo Spa | New aryl-and heteroarylethenylene derivatives and process for their preparation |
| US5912410A (en) | 1990-06-15 | 1999-06-15 | Scios Inc. | Transgenic non-human mice displaying the amyloid-forming pathology of alzheimer's disease |
| JPH06507782A (ja) | 1990-06-15 | 1994-09-08 | サイオス ノバ インコーポレイテッド | アルツハイマー病のアミロイド形成開症状を示すヒト以外の組換え哺乳動物 |
| JPH05508855A (ja) | 1990-07-06 | 1993-12-09 | スミスクライン・ビーチャム・コーポレイション | レトロウイルスプロテアーゼ阻害剤 |
| US5482947A (en) | 1990-11-19 | 1996-01-09 | Talley; John J. | Retroviral protease inhibitors |
| US5648511A (en) | 1990-11-19 | 1997-07-15 | G.D. Searle & Co. | Method for making intermediates useful in the synthesis of retroviral protease inhibitors |
| US5708004A (en) | 1990-11-19 | 1998-01-13 | Monsanto Company | Retroviral protease inhibitors |
| CA2372251A1 (fr) | 1991-01-21 | 1992-08-06 | Michael John Mullan | Test et modele pour la maladie d'alzheimer |
| US5145684A (en) | 1991-01-25 | 1992-09-08 | Sterling Drug Inc. | Surface modified drug nanoparticles |
| US5206161A (en) | 1991-02-01 | 1993-04-27 | Genentech, Inc. | Human plasma carboxypeptidase B |
| WO1992017490A1 (fr) | 1991-04-04 | 1992-10-15 | The Upjohn Company | Composes contenant du phosphore et servant d'inhibiteurs de retrovirus |
| CA2102511A1 (fr) | 1991-05-14 | 1992-11-15 | Paul J. Higgins | Anticorps heteroconjugues pour le traitement de l'infection a vih |
| US5753652A (en) | 1991-07-03 | 1998-05-19 | Novartis Corporation | Antiretroviral hydrazine derivatives |
| ES2093237T3 (es) * | 1991-07-03 | 1996-12-16 | Ciba Geigy Ag | Derivados de hidrazina farmacologicamente activos y procedimiento para su obtencion. |
| IE922316A1 (en) | 1991-07-17 | 1993-01-27 | Smithkline Beecham Corp | Retroviral protease inhibitors |
| US5516784A (en) | 1991-08-13 | 1996-05-14 | Schering Corporation | Anti-HIV (AIDS) agents |
| WO1993008829A1 (fr) | 1991-11-04 | 1993-05-13 | The Regents Of The University Of California | Compositions induisant la destruction de cellules infectees par l'hiv |
| DK0620849T3 (da) | 1992-01-07 | 2003-10-20 | Elan Pharm Inc | Transgene dyremodeller for Alzheimer's sygdom |
| JPH07504417A (ja) | 1992-02-26 | 1995-05-18 | スミスクライン・ビーチャム・コーポレイション | レトロウイルスプロテアーゼ拮抗薬 |
| ATE253050T1 (de) | 1992-03-11 | 2003-11-15 | Narhex Ltd | Aminderivate von oxo- und hydroxy- substituierten kohlenwasserstoffen |
| DK0560268T3 (da) | 1992-03-13 | 1995-06-12 | Bio Mega Boehringer Ingelheim | Substituerede pipecolinsyrederivater som HIV-proteasehæmmere |
| US5502187A (en) | 1992-04-03 | 1996-03-26 | The Upjohn Company | Pharmaceutically active bicyclic-heterocyclic amines |
| US5604102A (en) | 1992-04-15 | 1997-02-18 | Athena Neurosciences, Inc. | Methods of screening for β-amyloid peptide production inhibitors |
| US5441870A (en) | 1992-04-15 | 1995-08-15 | Athena Neurosciences, Inc. | Methods for monitoring cellular processing of β-amyloid precursor protein |
| US5376542A (en) | 1992-04-27 | 1994-12-27 | Georgetown University | Method for producing immortalized cell lines using human papilluma virus genes |
| US5766846A (en) | 1992-07-10 | 1998-06-16 | Athena Neurosciences | Methods of screening for compounds which inhibit soluble β-amyloid peptide production |
| DK0656887T3 (da) | 1992-08-25 | 1999-07-05 | Searle & Co | Hydroxyethylaminosulfonamider til anvendelse som inhibitorer af retrovirale proteaser |
| KR100296462B1 (ko) | 1992-08-25 | 2001-10-24 | 죤 에이치. 뷰센 | 레트로바이러스프로테아제억제제로서유용한술포닐알칸오일아미노히드록시에틸아미노술폰아미드 |
| US5760076A (en) | 1992-08-25 | 1998-06-02 | G.D Searle & Co. | Succinoylamino hydroxyethylamino sulfonamides useful as retroviral protease inhibitors |
| US5830897A (en) | 1992-08-27 | 1998-11-03 | G. D. Searle & Co. | α- and β-amino acid hydroxyethylamino sulfonamides useful as retroviral protease inhibitors |
| US5578606A (en) | 1992-10-30 | 1996-11-26 | G. D. Searle & Co. | α- and β-amino acid hydroxyethylamino sulfonyl urea derivatives useful as retroviral protease inhibitors |
| MX9308025A (es) | 1992-12-22 | 1994-08-31 | Lilly Co Eli | Compuestos inhibidores de la proteasa del virus dela inmunodeficiencia humana, procedimiento para supreparacion y formulacion farmaceutica que los contiene. |
| DE69329544T2 (de) | 1992-12-22 | 2001-05-31 | Eli Lilly And Co., Indianapolis | HIV Protease hemmende Verbindungen |
| US5484926A (en) | 1993-10-07 | 1996-01-16 | Agouron Pharmaceuticals, Inc. | HIV protease inhibitors |
| US5461067A (en) * | 1993-02-25 | 1995-10-24 | Abbott Laboratories | Retroviral protease inhibiting compounds |
| ATE174587T1 (de) | 1993-08-24 | 1999-01-15 | Searle & Co | Hydroxyaminosulfonamide verwendbar als inhibitoren retroviraler proteasen |
| ATE198622T1 (de) | 1993-10-27 | 2001-01-15 | Elan Pharm Inc | Transgene tiere, die app allele mit der schwedischen mutation beherbergen |
| JPH07126286A (ja) | 1993-11-05 | 1995-05-16 | Yamanouchi Pharmaceut Co Ltd | 新規なペプチド誘導体 |
| US5733882A (en) | 1994-01-17 | 1998-03-31 | Smithkline Beecham Corporation | Retroviral protease inhibitors |
| US5877399A (en) | 1994-01-27 | 1999-03-02 | Johns Hopkins University | Transgenic mice expressing APP-Swedish mutation develop progressive neurologic disease |
| US5625031A (en) | 1994-02-08 | 1997-04-29 | Bristol-Myers Squibb Company | Peptide inhibitors of the p33cdk2 and p34cdc2 cell cycle regulatory kinases and human papillomavirus E7 oncoprotein |
| US5475138A (en) | 1994-07-07 | 1995-12-12 | Pharm-Eco Laboratories Incorporated | Method preparing amino acid-derived diaminopropanols |
| DK0708085T3 (da) | 1994-10-19 | 2002-11-11 | Novartis Ag | Antivirale ethere af aspartatproteasesubstrat-isostere |
| US6001813A (en) | 1994-11-21 | 1999-12-14 | Cortech Inc. | Val-pro containing α-keto oxadiazoles as serine protease inhibitors |
| AUPM982594A0 (en) * | 1994-12-02 | 1995-01-05 | University Of Queensland, The | HIV protease inhibitors |
| US5481011A (en) | 1994-12-13 | 1996-01-02 | Bristol-Myers Squibb Company | Process for preparing N-protected amino acid α-halomethyl ketones and alcohols from N-protected amino acid esters |
| US5863902A (en) | 1995-01-06 | 1999-01-26 | Sibia Neurosciences, Inc. | Methods of treating neurodegenerative disorders using protease inhibitors |
| US5804560A (en) | 1995-01-06 | 1998-09-08 | Sibia Neurosciences, Inc. | Peptide and peptide analog protease inhibitors |
| AU4700896A (en) | 1995-01-20 | 1996-08-07 | G.D. Searle & Co. | Bis-sulfonamide hydroxyethylamino retroviral protease inhibitors |
| US5831117A (en) | 1995-01-20 | 1998-11-03 | G. D. Searle & Co. | Method of preparing retroviral protease inhibitor intermediates |
| EP0805816B1 (fr) | 1995-01-27 | 2004-07-28 | Novo Nordisk A/S | Composes ayant des proprietes de liberation de l'hormone de croissance |
| US5545640A (en) | 1995-04-04 | 1996-08-13 | Bio-Mega/Boehringer Ingeleheim Research Inc. | Protease inhibiting succinic acid derivatives |
| TW493991B (en) | 1995-05-08 | 2002-07-11 | Novartis Ag | Pharmaceutical composition for oral administration of active agent having low water solubility and process for preparation of the same |
| US5744346A (en) | 1995-06-07 | 1998-04-28 | Athena Neurosciences, Inc. | β-secretase |
| US5565483A (en) | 1995-06-07 | 1996-10-15 | Bristol-Myers Squibb Company | 3-substituted oxindole derivatives as potassium channel modulators |
| US5942400A (en) | 1995-06-07 | 1999-08-24 | Elan Pharmaceuticals, Inc. | Assays for detecting β-secretase |
| DE69621651T2 (de) * | 1995-11-21 | 2002-11-21 | Novartis Ag, Basel | Azahexan-derivate als substratisostere von retroviralen aspartat-proteasen |
| US5886046A (en) | 1996-01-19 | 1999-03-23 | The Trustees Of The University Of Pennsylvania | Dicarbonyl-containing compounds |
| US5849691A (en) | 1996-02-20 | 1998-12-15 | The United States Of America As Represented By The Department Of Health And Human Services | Peptidomimetic inhibitors of cathepsin D and plasmepsins I and II |
| US5849911A (en) | 1996-04-22 | 1998-12-15 | Novartis Finance Corporation | Antivirally active heterocyclic azahexane derivatives |
| EP0901480A4 (fr) | 1996-05-07 | 1999-11-24 | Boehringer Ingelheim Pharma | Procede pour preparer des derives d'oxiranemethanamine |
| EP0923539B1 (fr) | 1996-07-22 | 2002-06-05 | Novo Nordisk A/S | Compositions favorisant la secretion d'hormone de croissance |
| US5914333A (en) | 1996-07-31 | 1999-06-22 | Novo Nordisk A/S | Treatment of psychotic disorders |
| US5703129A (en) | 1996-09-30 | 1997-12-30 | Bristol-Myers Squibb Company | 5-amino-6-cyclohexyl-4-hydroxy-hexanamide derivatives as inhibitors of β-amyloid protein production |
| WO1998022597A2 (fr) | 1996-11-20 | 1998-05-28 | Oklahoma Medical Research Foundation | Clonage et caracterisation de napsine, une protease aspartique |
| US6191166B1 (en) | 1997-11-21 | 2001-02-20 | Elan Pharmaceuticals, Inc. | Methods and compounds for inhibiting β-amyloid peptide release and/or its synthesis |
| US6153652A (en) | 1996-11-22 | 2000-11-28 | Elan Pharmaceuticals, Inc. | N-(aryl/heteroaryl/alkylacetyl) amino acid amides, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds |
| US6127556A (en) | 1996-12-31 | 2000-10-03 | G. D. Searle & Co. | Epoxide formation by continuous in-situ synthesis process |
| US6045829A (en) | 1997-02-13 | 2000-04-04 | Elan Pharma International Limited | Nanocrystalline formulations of human immunodeficiency virus (HIV) protease inhibitors using cellulosic surface stabilizers |
| DK0966443T3 (da) | 1997-02-26 | 2009-03-09 | Pfizer | Heteroaryl-hexansyre amidderivater, deres fremstilling og deres anvendelse som selektive inhibitorer af MIP-1-alfa binding til dens CCR1 receptor |
| US6221670B1 (en) | 1997-03-21 | 2001-04-24 | Scios Inc. | Methods to identify β-amyloid reducing agents |
| IL132630A0 (en) | 1997-05-08 | 2001-03-19 | Smithkline Beecham Corp | Protease inhibitors |
| US5962506A (en) | 1997-07-07 | 1999-10-05 | Pharmacopeia, Inc. | Glycol and hydroxyphosphonate peptidomimetics as inhibitors of aspartyl proteases |
| US6087383A (en) | 1998-01-20 | 2000-07-11 | Bristol-Myers Squibb Company | Bisulfate salt of HIV protease inhibitor |
| WO1999041266A1 (fr) | 1998-02-12 | 1999-08-19 | Emory University | Derives de sphingolipides et procedes d'utilisation |
| DE19817461A1 (de) | 1998-04-20 | 1999-10-21 | Basf Ag | Neue substituierte Benzamide, deren Herstellung und Anwendung |
| NZ508855A (en) * | 1998-06-19 | 2003-10-31 | Vertex Pharma | Sulfonamide inhibitors of HIV aspartyl protease |
| KR20060111905A (ko) | 1998-09-24 | 2006-10-30 | 파마시아 앤드 업존 캄파니 엘엘씨 | 알츠하이머병 세크레타제 |
| CA2359785A1 (fr) | 1999-02-10 | 2000-08-17 | John P. Anderson | Compositions a base d'enzyme .beta.-secretase et procedes |
| EP1178800A4 (fr) | 1999-03-24 | 2002-07-31 | Univ California | Traitement des maladies neurodegeneratives par des inhibiteurs de l'aspartyl protease |
| AU4072200A (en) | 1999-04-09 | 2000-11-14 | Human Genome Sciences, Inc. | 48 human secreted proteins |
| US7087399B1 (en) | 1999-05-13 | 2006-08-08 | Scios, Inc. | β-secretase and modulation of β-secretase activity |
| AU5619400A (en) | 1999-06-15 | 2001-01-02 | Elan Pharmaceuticals, Inc. | Statine-derived tetrapeptide inhibitors of beta-secretase |
| JP5138851B2 (ja) | 1999-06-28 | 2013-02-06 | オクラホマ メディカル リサーチ ファウンデーション | 触媒的に活性な組換えメマプシンおよびその使用方法 |
| EP1202737A4 (fr) | 1999-08-09 | 2005-03-02 | Univ Vanderbilt | Utilisation de modulateurs de p-glycoproteine dans un traitement antiviral |
| JP2003509411A (ja) | 1999-09-13 | 2003-03-11 | デュポン ファーマシューティカルズ カンパニー | Aβタンパク質の産生阻害剤としてのヒドロキシアルカノイルアミノラクタムおよび関連構造体 |
| PE20010693A1 (es) | 1999-09-23 | 2001-06-24 | Upjohn Co | Metodo para la determinacion de actividad alfa-secretasa sobre la app |
| GB9924957D0 (en) | 1999-10-21 | 1999-12-22 | Smithkline Beecham Plc | Novel treatment |
| EP1285088A2 (fr) | 2000-01-13 | 2003-02-26 | Genset | Marqueurs bialleles derives de regions genomiques comportant des genes responsables de troubles du systeme nerveux central |
| PE20020276A1 (es) * | 2000-06-30 | 2002-04-06 | Elan Pharm Inc | COMPUESTOS DE AMINA SUSTITUIDA COMO INHIBIDORES DE ß-SECRETASA PARA EL TRATAMIENTO DE ALZHEIMER |
| US6846813B2 (en) * | 2000-06-30 | 2005-01-25 | Pharmacia & Upjohn Company | Compounds to treat alzheimer's disease |
| CA2410680A1 (fr) | 2000-06-30 | 2002-01-10 | Elan Pharmaceuticals, Inc. | Composes pour le traitement de la maladie d'alzheimer |
| CA2448084A1 (fr) * | 2001-05-22 | 2002-11-28 | Elan Pharmaceuticals, Inc. | Composes ethylamine hydroxyles aza |
| CA2448834A1 (fr) | 2001-06-01 | 2002-12-12 | Elan Pharmaceuticals, Inc. | Derives d'hydroxyalkylamines comme inhibiteurs de beta-secratase et leurs utilisations pour le traitement de la maladie d'alzheimer et de maladies similaires |
| IL161881A0 (en) * | 2001-11-08 | 2005-11-20 | Upjohn Co | N,N'-substituted-1,3-diamino-2-hydroxypropane derivatives |
-
2001
- 2001-06-29 CA CA002410680A patent/CA2410680A1/fr not_active Abandoned
- 2001-06-29 AU AU2001271686A patent/AU2001271686A1/en not_active Abandoned
- 2001-06-29 KR KR1020027018013A patent/KR20030058959A/ko not_active Abandoned
- 2001-06-29 WO PCT/US2001/020930 patent/WO2002002506A2/fr not_active Ceased
- 2001-06-29 EP EP01952352A patent/EP1299352B1/fr not_active Expired - Lifetime
- 2001-06-29 DE DE60112942T patent/DE60112942T2/de not_active Expired - Fee Related
- 2001-06-29 NZ NZ523005A patent/NZ523005A/en unknown
- 2001-06-29 BR BR0111980-0A patent/BR0111980A/pt not_active IP Right Cessation
- 2001-06-29 WO PCT/US2001/020856 patent/WO2002002518A2/fr not_active Ceased
- 2001-06-29 JP JP2002507763A patent/JP2004502665A/ja active Pending
- 2001-06-29 MX MXPA02012560A patent/MXPA02012560A/es active IP Right Grant
- 2001-06-29 AU AU2001273094A patent/AU2001273094A1/en not_active Abandoned
- 2001-06-29 CN CN01812058XA patent/CN1217920C/zh not_active Expired - Fee Related
- 2001-06-29 CA CA002410972A patent/CA2410972A1/fr not_active Abandoned
- 2001-06-29 AU AU2001273113A patent/AU2001273113A1/en not_active Abandoned
- 2001-06-29 AT AT01952352T patent/ATE314343T1/de not_active IP Right Cessation
- 2001-06-29 US US09/896,874 patent/US7034182B2/en not_active Expired - Fee Related
- 2001-06-29 AT AT01950719T patent/ATE302751T1/de not_active IP Right Cessation
- 2001-06-29 JP JP2002507762A patent/JP2004502664A/ja not_active Abandoned
- 2001-06-29 DE DE60116313T patent/DE60116313T2/de not_active Expired - Fee Related
- 2001-06-29 ES ES01952352T patent/ES2252257T3/es not_active Expired - Lifetime
- 2001-06-29 EP EP01950719A patent/EP1299349B1/fr not_active Expired - Lifetime
- 2001-06-29 ES ES01950719T patent/ES2248356T3/es not_active Expired - Lifetime
- 2001-06-29 WO PCT/US2001/020852 patent/WO2002002505A2/fr not_active Ceased
-
2002
- 2002-12-10 ZA ZA200209991A patent/ZA200209991B/en unknown
-
2003
- 2003-01-13 ZA ZA200300327A patent/ZA200300327B/en unknown
-
2006
- 2006-03-07 US US11/370,073 patent/US7432389B2/en not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0652009A1 (fr) * | 1993-08-09 | 1995-05-10 | Eli Lilly And Company | L'identification et l'utilisation des inhibiteurs de la protease aspartic |
| WO1998033795A1 (fr) * | 1997-02-04 | 1998-08-06 | The Regents Of The University Of California | Inhibiteurs de cathepsine d nanomolaires et non peptidiques |
Non-Patent Citations (1)
| Title |
|---|
| N. CHEVALLIER ET AL, BRAIN RESEARCH, vol. 750, no. 1/2, 1997, pages 11 - 19, XP000921314 * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8691833B2 (en) | 2007-02-23 | 2014-04-08 | Merck Sharp & Dohme Corp. | Heterocyclic aspartyl protease inhibitors |
| US8691831B2 (en) | 2007-02-23 | 2014-04-08 | Merck Sharp & Dohme Corp. | Heterocyclic aspartyl protease inhibitors |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| WO2002002505A3 (fr) | Composes pour le traitement de la maladie d'alzheimer | |
| WO2002002512A3 (fr) | Composes utiles pour traiter la maladie d'alzheimer | |
| WO2002002520A3 (fr) | Composants utilises dans le traitement de la maladie d'alzheimer | |
| WO2001070672A3 (fr) | Composes et methodes de traitement de la maladie d'alzheimer | |
| GB0005251D0 (en) | Therapeutic compounds | |
| CA2411468A1 (fr) | Mimiques de thrombopoietine | |
| TNSN04165A1 (en) | Substituted hydroxyethylamines | |
| WO2002088101A3 (fr) | Inhibiteurs de bace | |
| AU4086101A (en) | Sulphonamido-substituted bridged bicycloalkyl derivatives | |
| WO2001078711A3 (fr) | Utilisation d'inhibiteurs de phosphodiesterase specifique de gmp cyclique pour le traitement de la maladie de parkinson | |
| AU2002314914A1 (en) | Hydroxy alkyl amine derivatives as beta-secretase inhibitors and their use for the treatment of alzheimer's disease and similar diseases | |
| MXPA02011288A (es) | Tioacetamidas substituidas. | |
| AU3173301A (en) | Methods and compositions for treatment of alzheimer's disease by enhancing plasmin or plasmin-like activity | |
| AU2002315131A1 (en) | Aminediols as agents for the treatment of alzheimer's disease | |
| AU2002239765A1 (en) | Antibody pti-hs7 for treatment of alzheimer's disease and other amyloidoses and parkinson's disease | |
| WO2004028548A3 (fr) | Agents neuroprotecteurs | |
| EP1404326A4 (fr) | Methode de traitement de la maladie de parkinson | |
| EP1586556A3 (fr) | Composés pour le traitement de la maladie d'Alzheimer | |
| AU2001255439A1 (en) | Method of treating alzheimer's disease | |
| AU2002303988A1 (en) | Methods of treating alzheimer's disease | |
| WO2001039573A3 (fr) | Utilisation nouvelle d'agent tensio-actif du poumon | |
| AU2002346015A1 (en) | Beta-hydroxyamine derivatives useful in treatment of alzheimer's disease | |
| AU2002305706A1 (en) | Use of tripeptide gpe for treating or preventing symptoms of parkinson's disease | |
| AU2002345863A1 (en) | Use of bicyclo compounds for treating alzheimer's disease |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AK | Designated states |
Kind code of ref document: A2 Designated state(s): AE AG AL AM AT AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ CZ DE DE DK DK DM DZ EC EE EE ES FI FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ PL PT RO RU SD SE SG SI SK SK SL TJ TM TR TT TZ UA UG UZ VN YU ZA ZW |
|
| AL | Designated countries for regional patents |
Kind code of ref document: A2 Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG |
|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
| DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
| AK | Designated states |
Kind code of ref document: A3 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT TZ UA UG UZ VN YU ZA ZW |
|
| AL | Designated countries for regional patents |
Kind code of ref document: A3 Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 2410680 Country of ref document: CA |
|
| ENP | Entry into the national phase |
Ref country code: JP Ref document number: 2002 507762 Kind code of ref document: A Format of ref document f/p: F |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 2001950719 Country of ref document: EP |
|
| WWP | Wipo information: published in national office |
Ref document number: 2001950719 Country of ref document: EP |
|
| REG | Reference to national code |
Ref country code: DE Ref legal event code: 8642 |
|
| CFP | Corrected version of a pamphlet front page | ||
| CR1 | Correction of entry in section i |
Free format text: IN PCT GAZETTE 02/2002 DUE TO A TECHNICAL PROBLEM AT THE TIME OF INTERNATIONAL PUBLICATION, SOME INFORMATION WAS MISSING (81). THE MISSING INFORMATION NOW APPEARS IN THE CORRECTED VERSION Free format text: IN PCT GAZETTE 02/2002 DUE TO A TECHNICAL PROBLEM AT THE TIME OF INTERNATIONAL PUBLICATION, SOME INFORMATION WAS MISSING (81). THE MISSING INFORMATION NOW APPEARS IN THE CORRECTED VERSION |
|
| WWG | Wipo information: grant in national office |
Ref document number: 2001950719 Country of ref document: EP |